Virulence as a target for antimicrobial chemotherapy

被引:24
作者
Alksne, LE [1 ]
机构
[1] Wyeth Res, Pearl River, NY 10965 USA
关键词
antimicrobial chemotherapy; pathogenesis; virulence;
D O I
10.1517/13543784.11.8.1149
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Bacterial resistance to present day antibiotics has become a dangerous threat to public health. Consequently, the pharmaceutical industry must provide new agents and novel classes to combat bacterial disease and to stay a step ahead of the rapid evolution of bacterial resistance mechanisms. The need for novel antibacterials has resulted in a search for previously unexplored targets for chemotherapy, utilising the new techniques of genomics to identify them. Several targets currently under investigation are involved in the process of bacterial virulence. These targets are unique in that their inhibition, by definition, should interfere with the process of infection rather than with bacterial viability. If successful, virulence inhibition may represent a 'kinder, gentler' approach to chemotherapy in which the pathogen is disarmed rather than killed outright.
引用
收藏
页码:1149 / 1159
页数:11
相关论文
共 99 条
[1]   Bacterial virulence as a target for antimicrobial chemotherapy [J].
Alksne, LE ;
Projan, SJ .
CURRENT OPINION IN BIOTECHNOLOGY, 2000, 11 (06) :625-636
[2]   New antibiotic discovery, novel screens, novel targets and impact of microbial genomics [J].
Allsop, AE .
CURRENT OPINION IN MICROBIOLOGY, 1998, 1 (05) :530-534
[3]   Staphylococcus aureus bacteremia -: Consider the source. [J].
Archer, GL ;
Climo, MW .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (01) :55-56
[4]   Two-component signal transduction as a target for microbial anti-infective therapy [J].
Barrett, JF ;
Hoch, JA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (07) :1529-1536
[5]   Antibacterial agents that inhibit two-component signal transduction systems [J].
Barrett, JF ;
Goldschmidt, RM ;
Lawrence, LE ;
Foleno, B ;
Chen, R ;
Demers, JP ;
Johnson, S ;
Kanojia, R ;
Fernandez, J ;
Bernstein, J ;
Licata, L ;
Donetz, A ;
Huang, S ;
Hlasta, DJ ;
Macielag, MJ ;
Ohemeng, K ;
Frechette, R ;
Frosco, MB ;
Klaubert, DH ;
Whiteley, JM ;
Wang, L ;
Hoch, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (09) :5317-5322
[6]   How bacteria talk to each other: regulation of gene expression by quorum sensing [J].
Bassler, BL .
CURRENT OPINION IN MICROBIOLOGY, 1999, 2 (06) :582-587
[7]   INTERCELLULAR SIGNALING IN VIBRIO-HARVEYI - SEQUENCE AND FUNCTION OF GENES REGULATING EXPRESSION OF LUMINESCENCE [J].
BASSLER, BL ;
WRIGHT, M ;
SHOWALTER, RE ;
SILVERMAN, MR .
MOLECULAR MICROBIOLOGY, 1993, 9 (04) :773-786
[8]   MULTIPLE SIGNALING SYSTEMS CONTROLLING EXPRESSION OF LUMINESCENCE IN VIBRIO-HARVEYI - SEQUENCE AND FUNCTION OF GENES ENCODING A 2ND SENSORY PATHWAY [J].
BASSLER, BL ;
WRIGHT, M ;
SILVERMAN, MR .
MOLECULAR MICROBIOLOGY, 1994, 13 (02) :273-286
[9]  
Black T, 2000, CURR OPIN MICROBIOL, V3, P522, DOI 10.1016/S1369-5274(00)00133-8
[10]   Inactivation of the srtA gene in Streptococcus gordonii inhibits cell wall anchoring of surface proteins and decreases in vitro and in vivo adhesion [J].
Bolken, TC ;
Franke, CA ;
Jones, KF ;
Zeller, GO ;
Jones, CH ;
Dutton, EK ;
Hruby, DE .
INFECTION AND IMMUNITY, 2001, 69 (01) :75-80